Variant report

Variant	esv3342547
Chromosome Location	chr1:246646029-246649827
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:246647202-246648395	GM12878	blood:	n/a	n/a
2	BATF	chr1:246648136-246648477	GM12878	blood:	n/a	n/a
3	BCL11A	chr1:246647613-246648442	GM12878	blood:	n/a	n/a
4	CTCF	chr1:246648264-246648313	GM10248	blood:	n/a	n/a
5	CTCF	chr1:246648283-246648413	GM20000	blood:	n/a	n/a
6	CTCF	chr1:246648278-246648340	GM13976	blood:	n/a	n/a
7	EBF1	chr1:246646072-246646364	GM12878	blood:	n/a	chr1:246646214-246646225 chr1:246646243-246646254
8	EBF1	chr1:246648048-246648335	GM12878	blood:	n/a	n/a
9	EBF1	chr1:246647546-246647928	GM12878	blood:	n/a	n/a
10	EP300	chr1:246648005-246648635	GM12878	blood:	n/a	n/a
11	ESR1	chr1:246648100-246648550	T-47D	breast:	n/a	n/a
12	FOS	chr1:246646526-246646802	MCF10A-Er-Src	breast:	n/a	chr1:246646616-246646625 chr1:246646616-246646624 chr1:246646617-246646624
13	FOS	chr1:246646455-246646813	MCF10A-Er-Src	breast:	n/a	chr1:246646616-246646625 chr1:246646616-246646624 chr1:246646617-246646624
14	FOSL2	chr1:246648087-246648498	HepG2	liver:	n/a	n/a
15	FOXA1	chr1:246647249-246647598	HepG2	liver:	n/a	n/a
16	FOXA1	chr1:246647715-246648258	HepG2	liver:	n/a	n/a
17	GATA2	chr1:246647691-246648472	K562	blood:	n/a	n/a
18	IRF4	chr1:246647182-246648490	GM12878	blood:	n/a	n/a
19	IRF4	chr1:246648173-246648554	GM12878	blood:	n/a	n/a
20	JUND	chr1:246646493-246646748	HepG2	liver:	n/a	chr1:246646616-246646625 chr1:246646616-246646624 chr1:246646614-246646625 chr1:246646617-246646624
21	JUND	chr1:246646064-246647096	SK-N-SH	brain:	n/a	chr1:246646616-246646625 chr1:246646616-246646624 chr1:246646614-246646625 chr1:246646617-246646624
22	PAX5	chr1:246648076-246648544	GM12878	blood:	n/a	n/a
23	PAX5	chr1:246648122-246648416	GM12878	blood:	n/a	n/a
24	PAX5	chr1:246647127-246648591	GM12878	blood:	n/a	n/a
25	POLR2A	chr1:246648074-246648447	GM12878	blood:	n/a	n/a
26	POLR2A	chr1:246648064-246648481	Hela-S3	cervix:	n/a	n/a
27	POU2F2	chr1:246647992-246648517	GM12878	blood:	n/a	n/a
28	RXRA	chr1:246647693-246647918	HepG2	liver:	n/a	n/a
29	RXRA	chr1:246647531-246648063	GM12878	blood:	n/a	n/a
30	SIX5	chr1:246647900-246648507	K562	blood:	n/a	n/a
31	SIX5	chr1:246647193-246647710	GM12878	blood:	n/a	n/a
32	SP1	chr1:246647474-246648654	GM12878	blood:	n/a	n/a
33	SP1	chr1:246647381-246648061	GM12878	blood:	n/a	n/a
34	STAT3	chr1:246646083-246646096	MCF10A-Er-Src	breast:	n/a	n/a
35	ZBTB33	chr1:246647961-246648549	K562	blood:	n/a	n/a
36	ZBTB33	chr1:246647951-246648337	K562	blood:	n/a	n/a
37	ZBTB33	chr1:246647333-246647947	HepG2	liver:	n/a	n/a
38	ZBTB33	chr1:246647561-246647925	K562	blood:	n/a	n/a
39	ZBTB33	chr1:246648094-246648425	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246646424-246646474	BJ	skin:	n/a
2	chr1:246646424-246646474	AG10803	skin:	n/a
3	chr1:246646424-246646474	HEK293	kidney:	embryo
4	chr1:246646424-246646474	AG04450	lung:	fetal
5	chr1:246646424-246646474	H1-hESC	embryonic stem cell:	embryo
6	chr1:246646424-246646474	AG04449	skin:	fetal
7	chr1:246646424-246646474	CMK	blood:	n/a
8	chr1:246646424-246646474	RPTEC	kidney:	n/a
9	chr1:246646424-246646474	HUVEC	blood vessel:	n/a
10	chr1:246646424-246646474	GM12878	blood:	n/a
11	chr1:246646424-246646474	HCF	heart:	n/a
12	chr1:246646424-246646474	PANC-1	pancreas:	n/a
13	chr1:246646424-246646474	HCPEpiC	choroid plexus:	n/a
14	chr1:246646424-246646474	SAEC	small airway:	n/a
15	chr1:246646424-246646474	U87	brain:	n/a
16	chr1:246646424-246646474	A549	lung:	n/a
17	chr1:246646424-246646474	ECC-1	luminal epithelium:	n/a
18	chr1:246646424-246646474	NHDF-neo	bronchial:	n/a
19	chr1:246646424-246646474	SK-N-MC	brain:	n/a
20	chr1:246646424-246646474	ProgFib	skin:	n/a
21	chr1:246646424-246646474	HRCEpiC	kidney:	n/a
22	chr1:246646424-246646474	PrEC	prostate:	n/a
23	chr1:246646424-246646474	NB4	blood:	n/a
24	chr1:246646424-246646474	NT2-D1	testis:	n/a
25	chr1:246646424-246646474	HAEpiC	amniotic membrane:	n/a
26	chr1:246646424-246646474	PFSK-1	brain:	n/a
27	chr1:246646424-246646474	MCF10A-Er-Src	breast:	n/a
28	chr1:246646424-246646474	GM06990	blood:	n/a
29	chr1:246646424-246646474	HL-60	blood:	n/a
30	chr1:246646424-246646474	ovcar-3	ovarian:	n/a
31	chr1:246646424-246646474	HCT-116	colon:	n/a
32	chr1:246646424-246646474	Jurkat	blood:	n/a
33	chr1:246646424-246646474	BE2_C	brain:	n/a
34	chr1:246646424-246646474	NHBE	bronchial:	n/a
35	chr1:246646424-246646474	AoSMC	blood vessel:	n/a
36	chr1:246646424-246646474	Hela-S3	cervix:	n/a
37	chr1:246646424-246646474	IMR90	lung:	fetal
38	chr1:246646424-246646474	AG09319	gingival:	n/a
39	chr1:246646424-246646474	LNCaP	prostate:	n/a
40	chr1:246646424-246646474	HRPEpiC	eye:	n/a
41	chr1:246646424-246646474	HRE	kidney:	n/a
42	chr1:246646424-246646474	SK-N-SH_RA	brain:	n/a
43	chr1:246646424-246646474	Hepatocyte	liver:	n/a
44	chr1:246646424-246646474	HNPCEpiC	eye:	n/a
45	chr1:246646424-246646474	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:246646424-246646474	SK-N-SH	brain:	n/a
47	chr1:246646424-246646474	HEEpiC	esophagus:	n/a
48	chr1:246646424-246646474	AG09309	skin:	n/a
49	chr1:246646424-246646474	HMEC	breast:	n/a
50	chr1:246646424-246646474	K562	blood:	n/a

No data

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3	CpG island

Extended variants
information (count: 222 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:222 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568697295	chr1:246646046-246646047	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs142210786	chr1:246646055-246646056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs188391434	chr1:246646097-246646098	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570785171	chr1:246646101-246646102	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs150883301	chr1:246646102-246646103	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs181217224	chr1:246646206-246646207	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs199730501	chr1:246646234-246646235	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs374221439	chr1:246646235-246646236	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs575916682	chr1:246646237-246646238	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs397781970	chr1:246646238-246646239	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs199830663	chr1:246646239-246646240	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs566210863	chr1:246646262-246646263	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7537318	chr1:246646270-246646271	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528954776	chr1:246646294-246646295	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs375920913	chr1:246646330-246646331	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs555116442	chr1:246646401-246646402	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs374782452	chr1:246646425-246646426	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs139332724	chr1:246646474-246646475	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs71638337	chr1:246646489-246646490	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs185061742	chr1:246646500-246646501	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188310293	chr1:246646523-246646524	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs143975747	chr1:246646543-246646544	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs563304663	chr1:246646547-246646548	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs532019521	chr1:246646588-246646589	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs548919201	chr1:246646632-246646633	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs148636953	chr1:246646648-246646649	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs527888920	chr1:246646662-246646663	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113230420	chr1:246646758-246646759	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs7539985	chr1:246646803-246646804	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539958125	chr1:246646810-246646811	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs547742982	chr1:246646851-246646852	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs549743024	chr1:246646858-246646859	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs569738374	chr1:246646877-246646878	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs7540076	chr1:246646892-246646893	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs377757299	chr1:246646917-246646918	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs59789284	chr1:246646918-246646919	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs565823040	chr1:246646956-246646957	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs147767723	chr1:246646957-246646958	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs139783849	chr1:246646992-246646993	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs145281961	chr1:246647011-246647012	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs75482813	chr1:246647032-246647033	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs397958152	chr1:246647033-246647034	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369217926	chr1:246647049-246647050	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs182030358	chr1:246647100-246647101	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs543568378	chr1:246647122-246647123	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs187587447	chr1:246647159-246647160	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573693220	chr1:246647235-246647236	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs73134187	chr1:246647245-246647246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs192026047	chr1:246647268-246647269	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs150984658	chr1:246647271-246647272	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246621600-246646400	Weak transcription	Primary B cells from cord blood	blood
2	chr1:246623200-246646600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:246623600-246663200	Weak transcription	Primary T cells from cord blood	blood
4	chr1:246632400-246647000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:246640400-246646200	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr1:246640800-246646200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:246641200-246646200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:246641400-246646800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:246644200-246646200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:246644800-246648400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:246645400-246646200	Enhancers	Small Intestine	intestine
12	chr1:246645600-246646400	Enhancers	Esophagus	oesophagus
13	chr1:246645600-246647200	Enhancers	Primary B cells from peripheral blood	blood
14	chr1:246645800-246646200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:246645800-246646200	Enhancers	Ovary	ovary
16	chr1:246645800-246646400	Enhancers	Colon Smooth Muscle	Colon
17	chr1:246645800-246646400	Enhancers	Pancreas	Pancrea
18	chr1:246645800-246646400	Enhancers	NHLF	lung
19	chr1:246645800-246646800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:246645800-246647200	Enhancers	Fetal Stomach	stomach
21	chr1:246646000-246646200	Enhancers	NHDF-Ad	bronchial
22	chr1:246646000-246646400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr1:246646000-246646600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:246646000-246646600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:246646000-246646600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr1:246646000-246647000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:246646000-246647200	Flanking Active TSS	GM12878-XiMat	blood
28	chr1:246646200-246646400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:246646200-246646400	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:246646200-246646400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:246646200-246646400	Flanking Active TSS	Ovary	ovary
32	chr1:246646200-246646400	Flanking Active TSS	Rectal Smooth Muscle	rectum
33	chr1:246646200-246646400	Enhancers	HSMM	muscle
34	chr1:246646200-246646400	Enhancers	Osteobl	bone
35	chr1:246646200-246646600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:246646200-246647000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:246646200-246647000	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr1:246646200-246647000	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr1:246646200-246647000	Flanking Active TSS	NHDF-Ad	bronchial
40	chr1:246646200-246647200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:246646200-246647200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:246646200-246647200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:246646200-246647200	Enhancers	Fetal Lung	lung
44	chr1:246646200-246647200	Active TSS	Stomach Smooth Muscle	stomach
45	chr1:246646200-246647400	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr1:246646400-246646600	Active TSS	Rectal Smooth Muscle	rectum
47	chr1:246646400-246646600	Flanking Active TSS	NHLF	lung
48	chr1:246646400-246646800	Enhancers	Primary B cells from cord blood	blood
49	chr1:246646400-246646800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr1:246646400-246646800	Enhancers	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links